The Recall Desk

State

Minnesota product recalls

73,827 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,851
Critical
1,137
Severe
2,246
Most recent
2026-11-04

Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53101–53125 of 81678

  • SevereFDA (Drugs)·D-1368-2016·2016-07-27

    PharMEDium Recalls Bupivacaine HCl Injectable Bags Due to Glass Particulates

    PharMEDium Services, LLC is recalling 2,874 bags of 0.25% Bupivacaine HCl injectable solution because the active ingredient was contaminated with glass particulate matter.

    Product
    0.25% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride; , Service Code 2H8120 , NDC 61553-120-50 , 250 ml in 250 ml Hospira LifeCare Bag ; , Service Code 2H8243 , NDC 61553-243-54 , 200 ml in 250 ml Hospira LifeCare Bag ; , Service Code 2K8120 , NDC 61553-120-09…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1408-2016·2016-07-27

    PharMEDium Recalls Fentanyl and Bupivacaine Bags Due to Glass Particulates

    PharMEDium Services is recalling 10 bags of compounded fentanyl and bupivacaine injectable solution because the active ingredient was contaminated with glass particulate matter.

    Product
    20 mcg/mL Fentanyl Citrate and 0.125% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride, 100 mL in 150 mL Baxter Intravia Bag, Service Code 2K8146, Rx Only, Compounded by PharMEDium Services, LLC, Memphis, TN 36141, NDC 61553-189-48
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1399-2016·2016-07-27

    PharMEDium Recalls Fentanyl and Bupivacaine Infusions Due to Glass Particulates

    PharMEDium Services, LLC is recalling 21 cassettes of compounded fentanyl and bupivacaine infusions because the active ingredient was contaminated with glass particulate matter.

    Product
    2 mcg/mL Fentanyl Citrate and 0.162% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride, 250 mL in 250 mL Yellow Smiths Medical Cassette, flow stop free flow-flow protection, Service Code 2T8229, Rx Only, Compounded by PharMEDium Services, LLC, Memphis, TN 36141, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1434-2016·2016-07-27

    PharMEDium Recalls Sterile Injectable Drugs Contaminated with Glass Particulate Matter

    PharMEDium Services is recalling 650 bags of sterile injectable drugs containing hydromorphone and bupivacaine due to the presence of glass particulate matter.

    Product
    8 mcg/mL HYDROmorphone HCl and 0.05% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride, 250 mL in 250 mL Hospira LifeCare Bag, Service Code 2H9310, Rx Only, Compounded by PharMEDium Services, LLC, Memphis, TN 36141, NDC 61553-310-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1409-2016·2016-07-27

    Pharmedium Recalls Hydrocodone and Bupivacaine Syringes Due to Glass Particulates

    Pharmedium Services is recalling 435 syringes of compounded hydrocodone and bupivacaine due to glass particulate contamination.

    Product
    20 mcg/mL HYDROmorphone HCl and 0.06% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride; 55 mL in 60 mL Monoject Syringe, Service Code 2T6620, Rx Only, Compounded by PharMEDium Services, LLC, Memphis, TN 36141, NDC 61553-620-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1376-2016·2016-07-27

    PharMEDium Recalls Sufentanil and Bupivacaine Bags Due to Glass Particulate

    PharMEDium Services, LLC is recalling 25 bags of compounded Sufentanil and Bupivacaine injectable solution because the active ingredient was contaminated with glass particulate.

    Product
    1 mcg/mL Sufentanil Citrate and 0.1% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride, 100 ml in 100 ml Hospira LifeCare Bag, Service Code 2H8919, Rx Only, Compounded by PharMEDium Services, LLC, Memphis, TN 36141, NDC 61553-0919-52
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2219-2016·2016-07-27

    WalkMed Infusion Pumps Recalled for Unapproved Software and Specification Changes

    WalkMed Infusion is voluntarily recalling Triton and Triton FP infusion pumps due to unapproved changes to software, specifications, and intended use.

    Product
    The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1727-2016·2016-07-27

    Kellogg Recalls Famous Amos Cookies Due to Undeclared Peanut Allergen

    Kellogg Company is voluntarily recalling Famous Amos Cookies Double Chocolate Chip because of a potential undeclared peanut allergen resulting from a supplier's flour recall.

    Product
    Famous Amos Cookies Double Chocolate Chip, 12 ct., 12.4 oz.
    Category
    Food
    Distribution
    46 states
  • HighFDA (Devices)·Z-2234-2016·2016-07-27

    WalkMed Infusion Recalls IV Sets Due to Potential Particulate Presence

    WalkMed Infusion is voluntarily recalling specific lots of Triton IV administration sets due to the potential presence of particulate matter in or on the devices.

    Product
    T105-000WC IV Set w/2 Y-Sites, BC Vlv & Filter Cap. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1723-2016·2016-07-27

    Kellogg Recalls Keebler Frozen Graham Snacks Cinnamon for Undeclared Peanut

    Kellogg Company is voluntarily recalling Keebler Frozen Graham Snacks Cinnamon due to the potential for undeclared peanut allergen resulting from a supplier's flour recall.

    Product
    Keebler Frozen Graham Snacks Cinnamon, 4 ct., 12.7 oz. ; and cups 2.2 oz. 10 ct., and cups 2.2 oz. 8 ct.
    Category
    Food
    Distribution
    46 states
  • HighCPSC·16762·2016-07-27

    Emson Recalls UComfy Neck and Shoulder Heat Wraps Due to Burn Hazard

    Emson is recalling UComfy Neck and Shoulder Heat Wraps because they can overheat and cause burns. Consumers should stop using the product and contact Emson for a free replacement.

    Product
    UComfy Neck and Shoulder Heat Wrap
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1732-2016·2016-07-27

    Keebler Mini Sandies Shortbread Cookies Recalled for Undeclared Peanut

    Kellogg Company is recalling Keebler Mini Sandies Shortbread cookies due to potential undeclared peanut allergen from a flour supplier issue.

    Product
    Keebler Mini Sandies Shortbread cookies, 100 ct., 1.0 oz.
    Category
    Food
    Distribution
    46 states
  • HighFDA (Food)·F-1724-2016·2016-07-27

    Kellogg Recalls Keebler Fudge Cookies Due to Undeclared Peanut Allergen

    Kellogg Company is voluntarily recalling Keebler E. L. Fudge Double Stuffed Sandwich Cookies because they may contain undeclared peanut.

    Product
    Keebler E. L. Fudge Double Stuffed Sandwich Cookies, 12 ct., 12 oz.
    Category
    Food
    Distribution
    46 states
  • HighFDA (Food)·F-1736-2016·2016-07-27

    Kellogg Recalls Gripz Variety Packs Due to Undeclared Peanut Allergen

    Kellogg Company is voluntarily recalling Gripz Variety On the Go Packs because they may contain undeclared peanut, a common allergen, due to a supplier's flour recall.

    Product
    Gripz Variety On the Go Pack, 14 pack, 12.6 oz.
    Category
    Food
    Distribution
    46 states
  • HighFDA (Food)·F-1733-2016·2016-07-27

    Kellogg Recalls Famous Amos Chocolate Chip Cookies for Undeclared Peanut

    Kellogg Company is voluntarily recalling Famous Amos Chocolate Chip Cookies due to potential undeclared peanut allergen from a flour supplier issue.

    Product
    Famous Amos Cookies Chocolate Chip, 12 ct., 12.4 oz.; and 2.7 oz. cup
    Category
    Food
    Distribution
    46 states
  • HighFDA (Devices)·Z-2221-2016·2016-07-27

    WalkMed Infusion Recalls Spike Sets Due to Potential Particulate Presence

    WalkMed Infusion is voluntarily recalling 12-inch Microbore Spike Sets due to the potential presence of particulate matter in or on the devices.

    Product
    Spike Set, 12" Microbore SPM-12. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1737-2016·2016-07-27

    Kellogg Recalls Keebler Animal Totes for Undeclared Peanut Allergen

    Kellogg Company is voluntarily recalling Keebler Animal Totes due to a potential undeclared peanut allergen resulting from a supplier's flour recall.

    Product
    Keebler Animal Totes, bulk tote 400 lb.
    Category
    Food
    Distribution
    46 states
  • HighFDA (Drugs)·D-1364-2016·2016-07-27

    PharMEDium Recalls Bupivacaine HCl Injectable Bags Due to Glass Particulate

    PharMEDium Services is recalling 4,081 bags of 0.1% Bupivacaine HCl injectable solution because the active ingredient was contaminated with glass particulate matter.

    Product
    0.1% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride, Service Code 2K8195, 100 ml in 150 ml Baxter Intravia Bag (NDC 61553-195-48), Service Code 2H8266, 250 ml in 250 ml Hospira LifeCare Bag NDC 61553-266-50), 100 ml in 100 ml Hospira LifeCare Bag, Service Code…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2232-2016·2016-07-27

    WalkMed Infusion Recalls Triton Administration Sets Due to Particulate Presence

    WalkMed Infusion is voluntarily recalling Triton Administration Sets because they may contain particulate matter. The recall affects 383 cases distributed nationwide.

    Product
    T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide